A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548692



Internal ID21873047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55951377..55951377hg38UCSC Ensembl
chr5:55247205..55247205hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076668
Supporting Variants
Samples
Known GenesIL6ST
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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